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22935002: Congenital erythropoietic porphyria (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

38524015 Congenital erythropoietic porphyria en Synonym Active Entire term case insensitive SNOMED CT core module

38525019 Gunther's disease en Synonym Active Entire term case sensitive SNOMED CT core module

38526018 Congenital photosensitive porphyria en Synonym Active Entire term case insensitive SNOMED CT core module

38528017 Hematoporphyria congenita en Synonym Active Entire term case insensitive SNOMED CT core module

38529013 Porphyria erythropoietica en Synonym Active Entire term case insensitive SNOMED CT core module

481477016 Haematoporphyria congenita en Synonym Active Entire term case insensitive SNOMED CT core module

752399013 Congenital erythropoietic porphyria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1223000017 Uroporphyrinogen III synthase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

1223001018 CEP - Congenital erythropoietic porphyria en Synonym Active Entire term case sensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital erythropoietic porphyria	Is a	Erythropoietic porphyria	true	Inferred relationship	Existential restriction modifier
Congenital erythropoietic porphyria	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Congenital erythropoietic porphyria	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Congenital erythropoietic porphyria	Is a	Congenital porphyria	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
38524015	Congenital erythropoietic porphyria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
38525019	Gunther's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
38526018	Congenital photosensitive porphyria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
38528017	Hematoporphyria congenita	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
38529013	Porphyria erythropoietica	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
481477016	Haematoporphyria congenita	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
752399013	Congenital erythropoietic porphyria (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1223000017	Uroporphyrinogen III synthase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
1223001018	CEP - Congenital erythropoietic porphyria	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module